Qurient Co., Ltd.
KOSDAQ biotech spun off from Institut Pasteur Korea, developing oncology and antibiotic drugs plus a drug distribution business.
As of 2026-10-10, Qurient Co., Ltd. has 14 PubMed-indexed papers on record (counted by the MAA Company Index from its own matching of public databases).
Price
Change
Market cap
Business overview
Source: DART corporate disclosureFounded in 2008 and listed on KOSDAQ in 2016, Qurient Co., Ltd. is a drug development biotech spun off from the Institut Pasteur Korea to commercialize its research outcomes. Its pipeline includes the CDK7 inhibitor mocaciclib (Q901), the Axl/Mer/CSF1R triple inhibitor adrixetinib (Q702), the next-generation dual-payload ADC QP101, the antibiotic telacebec (Q203), and the atopic dermatitis drug Q301, alongside a prescription drug distribution business. The company is organized into an R&D division and a drug distribution division, co-develops Keytruda combination regimens with MSD, out-licensed telacebec to the TB Alliance in February 2023, and reported consolidated revenue of KRW 7.0 billion at end-2025 and KRW 9.1 billion at end-2024.
Products & technology
- Pharmaceutical distribution businessSale of prescription and over-the-counter drugs
Clinical trials
data.go.kr2 MFDS clinical trial authorisations · 2022–2023 (Phase 1/2 2)
- Phase 1/2Q901, 키트루다주2023-06-21
14 trial sites
- Phase 1/2Q702, 키트루다주2022-09-06
10 trial sites
Global clinical trials
ClinicalTrials.gov · sponsor-matchedPhase 1 · Recruiting · 2025-12 · NCT07138196
Phase 1/2 · Active not recruiting · 2023-01 · NCT05438420
Phase 1/2 · Recruiting · 2022-08 · NCT05394103
Phase 2 · Terminated · 2021-07 · NCT04847583
Phase 1 · Completed · 2020-11 · NCT04648254
Phase 2 · Completed · 2018-07 · NCT03563599
Phase 2 · Completed · 2018-06 · NCT03571620
Phase 1 · Completed · 2016-08 · NCT02858973
Phase 1 · Completed · 2015-08 · NCT02530710
Phase 2 · Completed · 2015-04 · NCT02426359
R&D and key agreements
Source: DART corporate disclosureMocaciclib(Q901) · 난소암, 전립선암, 유방암, 자궁내막암, 결장직장암, 소세포폐암 또는 췌장암 · 1/2상 진행중(단독/병용) · CDK7 inhibitor in Phase 1/2 (monotherapy/combination) trials in the US and Korea; co-developed with MSD as a Keytruda combination and used as the basis for the QP101 ADC
QP101 · 고형암 · 비임상(단독) · Next-generation dual-payload ADC based on a topoisomerase 1 inhibitor, in preclinical stage
Adrixetinib(Q702) - 진행형 고형암 · 진행형 고형암 · 1상 완료(단독), 미국 · Axl/Mer/CSF1R triple inhibitor
Adrixetinib(Q702) - 이식편대숙주질환/희귀혈액암 · 만성 이식편대숙주질환, 희귀 혈액암 · 1상 진행중(단독), 미국 · Axl/Mer/CSF1R triple inhibitor
Adrixetinib(Q702) - 병용 고형암 · 위암, 식도암, 간암, 자궁경부암 · 1B/2상 진행중(병용), 미국·한국 · Developed as a Keytruda combination under a co-development agreement with MSD
Adrixetinib(Q702) - 급성 골수성 백혈병 · 급성 골수성 백혈병 · 1상 진행중(단독), 미국 · Axl/Mer/CSF1R triple inhibitor
Telacebec(Q203) · 다제내성결핵, 부룰리 궤양, 한센병 · 2/3상 진행중(단독), 미국·호주·남아공 · Cytochrome bc1 inhibitor; out-licensed to the TB Alliance in February 2023, began a registrational trial in Australia for Buruli ulcer in July 2024, dosing about 40 patients in 2024 and 100 in 2025; expected to be Qurient's first approved drug once the expanded trial completes
Q301 · 아토피성피부염 · 2B상 완료(단독), 미국 · Topical 5-LO inhibitor; various commercialization strategies under discussion based on Phase 2 efficacy results
Key disclosures
KRX KIND via OpenDART- Management투자판단관련주요경영사항(임상시험계획승인신청) (만성 이식편대숙주질환 환자 대상 Q702 단독치료요법의 유럽 임상 제1b상 임상시험계획 승인신청)2025-07-29
Publications
PubMed · affiliation-matched- Sensitizing tumor response to topoisomerase I antibody-drug conjugate by selective CDK7 inhibition.
Science advances · 2026-10 · Jung H, Lee Y, Yu D 외 13
- Sensitizing tumor response to topoisomerase I antibody drug conjugate by selective CDK7 inhibition.
bioRxiv : the preprint server for biology · 2025-11 · Jung H, Lee Y, Yu D 외 13
- The role of cytochrome bc1 inhibitors in future tuberculosis treatment regimens.
Nature communications · 2025-10 · Aguilar-Pérez C, Lenaerts AJ, Villellas C 외 34
- Telacebec, a Potent Agent in the Fight against Tuberculosis: Findings from a Randomized, Phase 2 Clinical Trial and Beyond.
American journal of respiratory and critical care medicine · 2025-08 · Janssen S, Upton C, de Jager VR 외 8
- Inhibition of AXL ameliorates pulmonary fibrosis via attenuation of M2 macrophage polarisation.
The European respiratory journal · 2025-06 · Kim DH, Kim HC, Im K 외 16
- An Antiherpesviral Host-Directed Strategy Based on CDK7 Covalently Binding Drugs: Target-Selective, Picomolar-Dose, Cross-Virus Reactivity.
Pharmaceutics · 2024-01 · Yu D, Wagner S, Schütz M 외 14
- Novel modeling approach integrating population pharmacokinetics and interspecies scaling to predict human pharmacokinetics of the new anti-tuberculosis agent telacebec (Q203).
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2023-11 · Kim J, Kim TH, Choi J 외 3
- Safety, Tolerability, Pharmacokinetics, and Metabolism of Telacebec (Q203) for the Treatment of Tuberculosis: a Randomized, Placebo-Controlled, Multiple Ascending Dose Phase 1B Trial.
Antimicrobial agents and chemotherapy · 2023-01 · Kim J, Choi J, Kang H 외 9
- A Novel Selective Axl/Mer/CSF1R Kinase Inhibitor as a Cancer Immunotherapeutic Agent Targeting Both Immune and Tumor Cells in the Tumor Microenvironment.
Cancers · 2022-10 · Jeon Y, Kang H, Yang Y 외 5
- Safety, Tolerability, and Pharmacokinetics of Telacebec (Q203), a New Antituberculosis Agent, in Healthy Subjects.
Antimicrobial agents and chemotherapy · 2022-01 · Kim J, Choi J, Kang H 외 9
Show 4 more publications
- Telacebec for Ultrashort Treatment of Buruli Ulcer in a Mouse Model.
Antimicrobial agents and chemotherapy · 2020-05 · Almeida DV, Converse PJ, Omansen TF 외 4
- Telacebec (Q203), a New Antituberculosis Agent.
The New England journal of medicine · 2020-03 · de Jager VR, Dawson R, van Niekerk C 외 7
- Synthesis and structure-activity relationships of novel fused ring analogues of Q203 as antitubercular agents.
European journal of medicinal chemistry · 2017-08 · Kang S, Kim YM, Jeon H 외 9
- Synthesis and structure-activity studies of side chain analogues of the anti-tubercular agent, Q203.
European journal of medicinal chemistry · 2017-01 · Kang S, Kim YM, Kim RY 외 5
Patents
KIPRIS · applicant-matchedCN · Published · 2023-08 · Application 202380070893.4
US · Published · 2023-08 · Application 19100289
EP · Published · 2023-08 · Application 23751933.5
PCT · Published · 2023-08 · Application PCT/EP2023/071458
Published · 2023-08 · Application 1020257007181
US · Published · 2023-03 · Application 18848272
EP · Published · 2023-03 · Application 23712868.1
PCT · Published · 2023-03 · Application PCT/EP2023/056950
- Subsidiary: QLi5 Therapeutics AGMacrocyclic compounds as proteasome beta subunit type 5 inhibitors
CN · Published · 2022-09 · Application 202280074659.4
- Subsidiary: QLi5 Therapeutics AGMACROCYCLIC COMPOUNDS AS PROTEASOME SUBUNIT BETA TYPE-5 INHIBITORS
US · Published · 2022-09 · Application 18694432
Show 79 more patents
- Subsidiary: QLi5 Therapeutics AGMACROCYCLIC COMPOUNDS AS PROTEASOME SUBUNIT BETA TYPE-5 INHIBITORS
EP · Registered · 2022-09 · Application 22797303.9
US · Published · 2022-05 · Application 18562676
PCT · Published · 2022-05 · Application PCT/EP2022/064443
CN · Published · 2022-03 · Application 202280094492.8
US · Published · 2022-03 · Application 18845270
EP · Published · 2022-03 · Application 22719858.7
PCT · Published · 2022-03 · Application PCT/EP2022/058450
Published · 2022-03 · Application 1020247030877
US · Registered · 2021-12 · Application 17548978
US · Registered · 2021-11 · Application 18036102
EP · Published · 2021-11 · Application 21819125.2
PCT · Published · 2021-11 · Application PCT/EP2021/083368
CN · Published · 2020-12 · Application 202080085924.X
US · Registered · 2020-12 · Application 17780969
EP · Registered · 2020-12 · Application 24176555.1
EP · Registered · 2020-12 · Application 20839277.9
PCT · Published · 2020-12 · Application PCT/EP2020/086772
Published · 2020-12 · Application 1020227021262
US · Registered · 2019-12 · Application 17787519
EP · Published · 2019-12 · Application 19832158.0
PCT · Published · 2019-12 · Application PCT/EP2019/087167
CN · Published · 2019-07 · Application 202511010051.7
US · Registered · 2019-07 · Application 17627928
EP · Published · 2019-07 · Application 24176134.5
EP · Registered · 2019-07 · Application 19756324.0
PCT · Published · 2019-07 · Application PCT/EP2019/070524
Registered · 2019-07 · Application 1020227004564
CN · Published · 2019-05 · Application 201980036560.3
EP · Published · 2019-05 · Application 19728645.3
US · Registered · 2019-05 · Application 17047961
PCT · Published · 2019-05 · Application PCT/EP2019/064214
Registered · 2019-05 · Application 1020207034321
EP · Published · 2019-04 · Application 19720424.1
CN · Published · 2019-04 · Application 201980039582.5
CN · Published · 2019-04 · Application 201980039675.8
EP · Published · 2019-04 · Application 19720425.8
US · Registered · 2019-04 · Application 17045030
US · Registered · 2019-04 · Application 17045009
PCT · Published · 2019-04 · Application PCT/EP2019/059302
PCT · Published · 2019-04 · Application PCT/EP2019/059289
Registered · 2019-04 · Application 1020207032379
Registered · 2019-04 · Application 1020207032377
US · Published · 2017-11 · Application 15816594
US · Registered · 2016-07 · Application 15215909
CN · Published · 2016-04 · Application 201680022317.2
EP · Registered · 2016-04 · Application 16716247.8
US · Registered · 2016-04 · Application 15563123
PCT · Published · 2016-04 · Application PCT/EP2016/058284
Registered · 2016-04 · Application 1020177032859
CN · Published · 2015-07 · Application 201580053161.X
EP · Registered · 2015-07 · Application 15748009.6
US · Registered · 2015-07 · Application 15327560
PCT · Published · 2015-07 · Application PCT/EP2015/067644
Registered · 2015-07 · Application 1020177005644
CN · Published · 2014-08 · Application 201480057004.1
EP · Registered · 2014-08 · Application 14858248.9
US · Registered · 2014-08 · Application 14777183
PCT · Published · 2014-08 · Application PCT/KR2014/007525
JP · Registered · 2014-08 · Application 28525982
Registered · 2014-08 · Application 1020140105106
CN · Published · 2014-08 · Application 201480054331.1
CN · Published · 2014-08 · Application 201811384685.9
EP · Registered · 2014-08 · Application 14745158.7
US · Published · 2014-08 · Application 14909663
PCT · Published · 2014-08 · Application PCT/EP2014/066614
Registered · 2014-08 · Application 1020167005457
Registered · 2014-07 · Application 1020140095974
Registered · 2014-07 · Application 1020140090425
Registered · 2014-07 · Application 1020140089737
Registered · 2014-07 · Application 1020140089260
Registered · 2014-07 · Application 1020140087020
Registered · 2014-07 · Application 1020140083691
Registered · 2014-07 · Application 1020140083726
Registered · 2014-07 · Application 1020140083200
Registered · 2014-07 · Application 1020140083210
Registered · 2013-10 · Application 1020130130165
PCT · Published · 2012-04 · Application PCT/IB2012/000991
Registered · 2012-04 · Application 1020197005476
Rejected · 2012-04 · Application 1020137030621
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Sources and updates
Counts on this page are not company-reported figures. MAA matched records from DART, the Korean MFDS, the US FDA, ClinicalTrials.gov, PubMed and KIPRIS to this company itself, by business registration number or registered name, never by name similarity. They may differ from figures the company publishes.
- Company basics
- Korea Exchange · DART
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- Compiled from disclosure filings
- Approvals & clinical trials
- Korean MFDS (data.go.kr) · US FDA openFDA — updated weekly
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- KRX KIND via OpenDART exchange filings — updated daily
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- Measured 2026-10-01
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